A Quercetin Containing Supplement Reduces Niacin-Induced Flush in Humans

Author:

Kalogeromitros D.1,Makris M.1,Chliva C.1,Aggelides X.1,Kempuraj D.2,Theoharides T.C.12345

Affiliation:

1. Allergy Clinical Research Center, Allergy Section, Attikon Hospital, University of Athens Medical School, Athens, Greece

2. Molecular Immunopharmacology and Drug Discovery Laboratory, Department of Pharmacology and Experimental Therapeutics

3. Department of Biochemistry, Tufts University School of Medicine, Medical Center, Boston, MA, USA

4. Department of Internal Medicine, Tufts University School of Medicine, Medical Center, Boston, MA, USA

5. Department of Psychiatry, Tufts University School of Medicine, Medical Center, Boston, MA, USA

Abstract

Coronary artery disease is associated with increased serum levels of cholesterol, triglycerides and LDL, but low levels of HDL. The most potent agent capable of reversing this trend is the vitamin nicotinic acid (niacin). However, compliance even with extended-release preparations and addition of acetylsalicylic acid (ASA) is hampered by the development of a feeling of erythema and burning (“flush”), especially on the face. We recently showed that the natural flavonoids quercetin and luteolin can eliminate “flush”, as well as inhibit both niacin-induced plasma prostaglandin D2 (PGD2) and serotonin increase in an animal model. We conducted a pilot clinical study in humans. Four normal male subjects received (a) 1 g immediate release niacin either alone or after (b) the dietary formulation (Algonot-plus®) containing 150 mg quercetin per capsule. Subjects completed a visual scale (1=no, 5=worst response) symptom assessment. Erythema and burning sensation scores were both 4.75±0.50 and lasted for 3.63±1.11 hours. After Algonot-plus® administration, both scores were reduced to 2.5±0.58 and lasted for only 1.68±0.70 hours. Quercetin also inhibited methylnicotinate-induced human mast cell PGD2 release. These preliminary results suggest that quercetin could reduce niacin-induced “flush” in humans.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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